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l-Dopa activation of RLM1 reporter in mpk1Δ strain. Wild-type strain (DL100) (▪) and the isogenic strain mpk1Δ (▴) were transformed with px2RLM1 and plated in 24-well plates on media containing the β-galactosidase substrate CPRG as described in Materials and Methods. l-Dopa was added to the media in increasing concentrations (0.1–0.5 mM), and β-galactosidase activity was measured at 570 nm after 48 h. Results shown are from five independent assays.
